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Nature Genetics|August 1, 1993
A duplication in the L1CAM gene associated with X-linked hydrocephalusG Van Camp, L Vits, P Coucke, et al.Nature Genetics|January 1, 1997
De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndromeT Matsuura, J S Sutcliffe, P Fang, et al.Nature Genetics|January 1, 1997
AP2 inhibits cancer cell growth and activates p21WAF1/CIP1 expressionY X Zeng, K Somasundaram, W S el-DeiryNature Genetics|January 1, 1997
Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysisA Hemminki, I Tomlinson, D Markie, et al.Nature Genetics|January 1, 1997
Low mutation rates of microsatellite loci in Drosophila melanogasterM D Schug, T F Mackay, C F AquadroNature Genetics|January 1, 1997
Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 geneS A Gayther, J Mangion, P Russell, et al.Nature Genetics|February 1, 1997
Mutation of HOXA13 in hand-foot-genital syndromeD P Mortlock, J W InnisNature Genetics|February 1, 1997
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndromeN Neyroud, F Tesson, I Denjoy, et al.Nature Genetics|February 1, 1997
Hypermutable myotonic dystrophy CTG repeats in transgenic miceD G Monckton, M I Coolbaugh, K T Ashizawa, et al.Nature Genetics|February 1, 1997
Men homozygous for an inactivating mutation of the follicle-stimulating hormone (FSH) receptor gene present variable suppression of spermatogenesis and fertilityJ S Tapanainen, K Aittomäki, J Min, et al.Pageof 744